Catalog

Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia

No MMS code

Link to WHO Definition

Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia – http://id.who.int/icd/entity/1252358703

Epilepsy due to a wide variety of clinical conditions having in common an X-linked genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.